GeneralAI / InformaticsDevice clearance
ANDI 2.2 — Imeka Solutions, Inc.
FDA 510(k) — Radiology devicesMay 28
FDA 510(k) clearance · Radiology · product code QIH
- Source: FDA 510(k) — Radiology devices (PRIMARY)
- Type: Device Clearance
RadPigeon summaries are original and for information only. They are not clinical advice.
